SH Ho Urology Centre, Division of Urology, Department of Surgery, The Chinese University of Hong Kong, Hong Kong, Hong Kong SAR.
Department of Urology, Erasmus MC, Rotterdam, The Netherlands.
Prostate Cancer Prostatic Dis. 2022 Apr;25(4):684-689. doi: 10.1038/s41391-021-00444-y. Epub 2021 Aug 27.
Men with elevated prostate-specific antigen (PSA) and initial negative prostate biopsy may have risk of prostate cancer (PCa) in the future. The role of Prostate Health Index (phi) in determining future PCa risk has not been studied before. This study aims to investigate the role of initial phi and phi density in predicting future PCa risk in men with initial negative biopsy.
Five hundred sixty nine men with PSA 4-10 ng/mL were recruited between 2008 and 2015 for prostate biopsy with prior phi. Electronic clinical record of men with initial negative biopsy was reviewed. Patients and follow-up doctors were blinded to phi. Kaplan-Meier curves were used to analyze the PCa-free survival in different baseline phi and phi density groups.
Four hundred sixty-one men with complete follow-up data were included. Median follow-up is 77 months. PCa and HGPCa was diagnosed in 8.2% (38/461) and 4.8% (22/461) of cohort respectively. A higher baseline phi value was associated with PCa (p = 0.003) and HGPCa (p < 0.001). HGPCa was diagnosed in 0.6% (1/163) of phi < 25, 4.6% (9/195) of phi 25-34.9, and 11.7% (12/103) of phi ≥ 35 (p < 0.001). HGPCa was diagnosed in 0% (0/109) and 21.0% (13/62) with phi density of <0.4 and ≥1.2, respectively, (p < 0.001). Kaplan-Meier curves showed phi and phi density predicted PCa and HGPCa diagnoses (log-rank test, all p ≤ 0.002).
Initial phi or phi density predicted 6-year risk of PCa in men with initial negative prostate biopsy. Men with higher phi (≥35) or phi density (≥1.2) need closer follow-up and repeated investigation, while men with lower phi (<25) or phi density (<0.4) could have less frequent follow-up.
前列腺特异性抗原(PSA)升高且初始前列腺活检阴性的男性未来可能患有前列腺癌(PCa)。Prostate Health Index(phi)在确定未来 PCa 风险方面的作用尚未得到研究。本研究旨在探讨初始 phi 和 phi 密度在预测初始阴性活检男性未来 PCa 风险中的作用。
2008 年至 2015 年间,招募了 569 名 PSA 为 4-10ng/ml 的男性进行前列腺活检,并在之前进行了 phi 检测。回顾了初始阴性活检男性的电子临床记录。患者和随访医生对 phi 均不知情。使用 Kaplan-Meier 曲线分析不同基线 phi 和 phi 密度组的 PCa 无进展生存率。
461 名男性有完整的随访数据。中位随访时间为 77 个月。该队列中分别诊断出 PCa 和 HGPCa 为 8.2%(38/461)和 4.8%(22/461)。较高的基线 phi 值与 PCa(p=0.003)和 HGPCa(p<0.001)相关。phi<25 的患者中,HGPCa 的诊断率为 0.6%(1/163),phi 为 25-34.9 的患者中为 4.6%(9/195),phi≥35 的患者中为 11.7%(12/103)(p<0.001)。phi 密度<0.4 和≥1.2 的患者中,HGPCa 的诊断率分别为 0%(0/109)和 21.0%(13/62)(p<0.001)。Kaplan-Meier 曲线显示 phi 和 phi 密度预测了 PCa 和 HGPCa 的诊断(对数秩检验,均 p≤0.002)。
初始 phi 或 phi 密度可预测初始阴性前列腺活检男性 6 年内 PCa 的发生风险。phi 值较高(≥35)或 phi 密度较高(≥1.2)的男性需要更密切的随访和重复检查,而 phi 值较低(<25)或 phi 密度较低(<0.4)的男性可以减少随访频率。